Clinical Data Manager: IQVIA x1 ( bloemfontein)
- Company: IQVIA
- Location: Bloemfontein, South Africa (Home-based)
- Other Locations: Bellville, Centurion, London, Reading
- Employment Type: Full-time
- Salary: R1,452,488 per annum
- Posted: 2026
Job Overview
The Clinical Data Manager (CDM) will provide scientific and complex clinical data review, collaborating closely with Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS). This role focuses on therapeutic areas such as Oncology, Cardiovascular (CV), and Immunology and ensures that clinical data management deliverables meet quality, regulatory, and study-specific requirements.
Main Responsibilities
Perform scientific (complex) clinical data review across one high complexity trial or multiple low-to-moderate complexity trials.
Collaborate with SRP, SRS, and Data Management teams to establish and confirm data review expectations.
Review protocols, data collection tools, and Data Management Plans from the protocol design stage.
Manage clinical data queries in the EDC system (Rave mandatory).
Conduct other review activities including coding, SAE reconciliation, and integrated review planning.
Lead or attend meetings as required, ensuring alignment with study objectives and CDM deliverables.
Set timelines for deliverables and track milestones to ensure on-time completion.
Create Integrated Review Plans ensuring accuracy, clarity, scientific content, and regulatory compliance.
Support inspection readiness for Regulatory Agency audits and client internal audits.
Identify and implement process, system, and tool improvement initiatives.
Provide lessons learned, best practices, and FAQs at the trial level.
Minimum Qualifications & Experience
BS/BA degree or higher in Health Sciences or a related field.
At least 5 years of clinical data management experience with scientific/complex data review.
Experience in eCRF build and Rave platform mandatory.
Knowledge of medical terminology preferred.
Proven experience collaborating with SRP/SRS and clinical teams in therapeutic areas: Oncology, Cardiovascular, and Immunology.
Familiarity with ICH-GCP, regulatory requirements, and SOPs.
Skills & Competencies
Strong leadership and collaboration skills within cross-functional teams.
Attention to detail and commitment to data quality and accuracy.
Ability to plan, track, and ensure timely delivery of CDM milestones.
Effective communication with study teams, clients, and vendors.
Problem-solving and analytical skills, with the ability to improve processes.
Company Overview
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. IQVIA accelerates the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
Committed to hiring integrity and maintains zero tolerance for candidate fraud.